Background: Neuroendocrine neoplasms (NENs) are slow-growing tumors. Sarcopenia is defined as the loss of muscle mass, strength, and physical performance. First-line NEN therapy is somatostatin analogs, which could be responsible for malabsorption conditions, such as pancreatic exocrine insufficiency (EPI) with underlying sarcopenia. Aim: Evaluate the prevalence of sarcopenia in patients with NENs at diagnosis and during follow-up. Methods: A retrospective single-center study was conducted, including patients with advanced intestinal NENs G1/G2 (excluded pancreatic NENs). CT scans were analyzed at diagnosis and after 6 months of therapy, and the skeletal muscle index was assessed. Results: A total of 30 patients (F:M = 6:24) were enrolled, with the following primary tumor sites: 25 in the ileum, 1 stomach, 2 jejunum, and 2 duodenum. At diagnosis, 20 patients (66.6%) showed sarcopenic SMI values, and 10 patients (33.3%) showed non-sarcopenic SMI values. At follow-up, three more patients developed sarcopenic SMI values. Statistical significance in relation to the presence of sarcopenia was found in the group of patients with carcinoid syndrome (p = 0.0178), EPI (p = 0.0018), and weight loss (p = 0.0001). Conclusion: Sarcopenia was present in 2/3 of the patients with advanced intestinal NENs at the diagnosis and during the follow-up. It is reasonable to consider this condition to improve clinical outcomes.

Sarcopenia in patients with advanced gastrointestinal well-differentiated neuroendocrine tumors / Romano, Elena; Polici, Michela; Marasco, Matteo; Lerose, Francesco; Dell'Unto, Elisabetta; Nardacci, Stefano; Zerunian, Marta; Iannicelli, Elsa; Rinzivillo, Maria; Laghi, Andrea; Annibale, Bruno; Panzuto, Francesco; Caruso, Damiano. - In: NUTRIENTS. - ISSN 2072-6643. - 16:14(2024). [10.3390/nu16142224]

Sarcopenia in patients with advanced gastrointestinal well-differentiated neuroendocrine tumors

Romano, Elena
Primo
;
Polici, Michela;Marasco, Matteo;Lerose, Francesco;Dell'Unto, Elisabetta;Nardacci, Stefano;Zerunian, Marta;Iannicelli, Elsa;Rinzivillo, Maria;Laghi, Andrea;Annibale, Bruno;Panzuto, Francesco
;
Caruso, Damiano
Ultimo
2024

Abstract

Background: Neuroendocrine neoplasms (NENs) are slow-growing tumors. Sarcopenia is defined as the loss of muscle mass, strength, and physical performance. First-line NEN therapy is somatostatin analogs, which could be responsible for malabsorption conditions, such as pancreatic exocrine insufficiency (EPI) with underlying sarcopenia. Aim: Evaluate the prevalence of sarcopenia in patients with NENs at diagnosis and during follow-up. Methods: A retrospective single-center study was conducted, including patients with advanced intestinal NENs G1/G2 (excluded pancreatic NENs). CT scans were analyzed at diagnosis and after 6 months of therapy, and the skeletal muscle index was assessed. Results: A total of 30 patients (F:M = 6:24) were enrolled, with the following primary tumor sites: 25 in the ileum, 1 stomach, 2 jejunum, and 2 duodenum. At diagnosis, 20 patients (66.6%) showed sarcopenic SMI values, and 10 patients (33.3%) showed non-sarcopenic SMI values. At follow-up, three more patients developed sarcopenic SMI values. Statistical significance in relation to the presence of sarcopenia was found in the group of patients with carcinoid syndrome (p = 0.0178), EPI (p = 0.0018), and weight loss (p = 0.0001). Conclusion: Sarcopenia was present in 2/3 of the patients with advanced intestinal NENs at the diagnosis and during the follow-up. It is reasonable to consider this condition to improve clinical outcomes.
2024
neuroendocrine neoplasm; somatostatine analog; sarcopenia
01 Pubblicazione su rivista::01a Articolo in rivista
Sarcopenia in patients with advanced gastrointestinal well-differentiated neuroendocrine tumors / Romano, Elena; Polici, Michela; Marasco, Matteo; Lerose, Francesco; Dell'Unto, Elisabetta; Nardacci, Stefano; Zerunian, Marta; Iannicelli, Elsa; Rinzivillo, Maria; Laghi, Andrea; Annibale, Bruno; Panzuto, Francesco; Caruso, Damiano. - In: NUTRIENTS. - ISSN 2072-6643. - 16:14(2024). [10.3390/nu16142224]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1717182
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